Literature DB >> 14296590

PRIMARY HYPERPARATHYROIDISM IN AN INFANT; REPORT OF A CASE.

B FRETHEIM, O GARDBORG.   

Abstract

Entities:  

Keywords:  BLOOD; BLOOD ALKALINE PHOSPHATASE; BONE AND BONES; CALCIUM; DIAGNOSIS, DIFFERENTIAL; ERGOCALCIFEROL; HYPERCALCEMIA; HYPERPARATHYROIDISM; INFANT, NEWBORN; INFANT, NEWBORN, DISEASES; MENTAL RETARDATION; PATHOLOGY; PHOSPHORUS; RADIOGRAPHY; RICKETS

Mesh：

Substances：

Year:  1965        PMID： 14296590

Source DB:  PubMed          Journal:  Acta Chir Scand        ISSN： 0001-5482


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  3 in total

1.  In vivo and in vitro characterization of neonatal hyperparathyroidism resulting from a de novo, heterozygous mutation in the Ca2+-sensing receptor gene: normal maternal calcium homeostasis as a cause of secondary hyperparathyroidism in familial benign hypocalciuric hypercalcemia.

Authors:  M Bai; S H Pearce; O Kifor; S Trivedi; U G Stauffer; R V Thakker; E M Brown; B Steinmann
Journal:  J Clin Invest       Date:  1997-01-01       Impact factor: 14.808

2.  Hypohyperparathyroidism: a model for renal osteodystrophy?

Authors:  B J Junor; N Edward
Journal:  Postgrad Med J       Date:  1981-06       Impact factor: 2.401

3.  Primary infantile hyperparathyroidism: clinical, laboratory, and radiographic features in 21 cases.

Authors:  F Eftekhari; D K Yousefzadeh
Journal:  Skeletal Radiol       Date:  1982       Impact factor: 2.199
  3 in total

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